Between stringent compliance such as Annex 1 and GMP requirements and the need for absolute precision at every step, the fill/finish process is a highly demanding balancing act. It’s one with high risk of inefficiency and delays, especially when scaling batch sizes or working with complex formulations.

The Eurofins BioPharma Product Testing (BPT) network of laboratories simplifies this critical stage of production. Our integrated aseptic & non-aseptic fill/finish services bring together analytical testing and GMP-compliant fill/finish capabilities all under one roof to save you time, reduce complexity, and provide the flexibility you need in early clinical phases.

Our facilities are highly equipped

We specialise in small batch GMP manufacturing from Phase I to commercial batches For high-quality aseptic processing, we offer compounding services in class A biosafety cabinets in class B cleanrooms or an ISO 5 BSC located within an ISO 7 cleanroom, utilising a precise sterile filtration system equipped with aseptic connectors to eliminate potential contamination associated with aseptic technique. Some of our facilities are equipped with the Vanrx Microcell™ Vial Filler, an advanced, gloveless, robotic isolator that minimises contamination risk and eliminates human intervention. 

We provide a fully integrated, EU Annex 1-compliant solution with 100% environmental monitoring and “first air” flow across critical zones. 

Your single-source partner

Eurofins BPT will manage your entire CMC process—from raw material testing, and fill/finish, to QC release testing. Our services are supported by a dedicated project manager, rapid timeline management and secure 24/7 data access via LabAccess® online platform.

Combining technical expertise with flexible service models and global reach enables the Eurofins BPT network to help you progress your product swiftly and safely to the next development stage.